Construction and next-generation sequencing analysis of a large phage-displayed V NAR single-domain antibody library from six naïve nurse sharks.

Autor:	Feng M; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Bian H; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Wu X; Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, USA., Fu T; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Fu Y; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Hong J; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Fleming BD; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA., Flajnik MF; Department of Microbiology and Immunology, University of Maryland Baltimore School of Medicine, Baltimore, MD, USA., Ho M; Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Jazyk:	angličtina
Zdroj:	Antibody therapeutics [Antib Ther] 2019 Jan; Vol. 2 (1), pp. 1-11. Date of Electronic Publication: 2018 Nov 07.
DOI:	10.1093/abt/tby011
Abstrakt:	Background: Shark new antigen receptor variable domain (V NAR ) antibodies can bind restricted epitopes that may be inaccessible to conventional antibodies. Methods: Here, we developed a library construction method based on polymerase chain reaction (PCR)-Extension Assembly and Self-Ligation (named "EASeL") to construct a large V NAR antibody library with a size of 1.2 × 10 10 from six naïve adult nurse sharks ( Ginglymostoma cirratum ). Results: The next-generation sequencing analysis of 1.19 million full-length V NAR s revealed that this library is highly diversified because it covers all four classical V NAR types (Types I-IV) including 11% of classical Type I and 57% of classical Type II. About 30% of the total V NAR s could not be categorized as any of the classical types. The high variability of complementarity determining region (CDR) 3 length and cysteine numbers are important for the diversity of V NAR s. To validate the use of the shark V NAR library for antibody discovery, we isolated a panel of V NAR phage binders to cancer therapy-related antigens, including glypican-3, human epidermal growth factor receptor 2 (HER2), and programmed cell death-1 (PD1). Additionally, we identified binders to viral antigens that included the Middle East respiratory syndrome (MERS) and severe acute respiratory syndrome (SARS) spike proteins. The isolated shark single-domain antibodies including Type I and Type II V NAR s were produced in Escherichia coli and validated for their antigen binding. A Type II V NAR (PE38-B6) has a high affinity (K d  = 10.1 nM) for its antigen. Conclusions: The naïve nurse shark V NAR library is a useful source for isolating single-domain antibodies to a wide range of antigens. The EASeL method may be applicable to the construction of other large diversity gene expression libraries.
Databáze:	MEDLINE
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